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Clinical Trials/NCT02087072
NCT02087072
Withdrawn
Not Applicable

COLLABORATIVE HOME VISITS TO REDUCE HOSPITAL READMISSIONS AND IMPROVE MEDICATION USE DURING TRANSITIONS OF CARE

Ohio State University1 site in 1 countryOctober 2013

Overview

Phase
Not Applicable
Intervention
Not specified
Conditions
Transitional Care Coordination
Sponsor
Ohio State University
Locations
1
Primary Endpoint
Hospital Readmission
Status
Withdrawn
Last Updated
3 years ago

Overview

Brief Summary

The primary objective is to develop a sustainable practice model emphasizing home visits by a collaborative physician and pharmacist team to decrease unplanned emergency department visits and hospital readmissions at 30 and 90 days for high-risk home bound patients. Secondary objectives include (1) tracking the number, type, and severity of adverse drug events (ADE) and potential adverse drug events (pADE) that occur following hospital discharge and (2) resolving any identified ADE and pADE within 7 days of hospital discharge.

Adult patients will be scheduled for a home visit by the Healthy at Home Columbus program at the time of hospital discharge. The home visit will occur within 7 days of hospital discharge and will consist of a complete hospital and medication review by a physician or nurse practitioner and a pharmacist (including all lab tests, imaging studies, medication changes, and proposed plan of care at the time of discharge). The investigators hypothesize these home visits will reduce 30 and 90 days hospital readmission rates and ED visits.

The number of emergency department visits and unplanned hospital readmissions will be tracked at 30 and 90 days following discharge from the hospitalization that led to study enrollment. A comparison cohort of patients discharged in the 12 months prior to study initiation will be used to compare the effectiveness of the home visit program. The number and type of adverse drug events (ADE) and potential adverse drug events (pADE) that occur during transitions of care will also be characterized. All ADE and pADE will be resolved during the initial home visit and will be classified based on severity. All ADE and pADE will be evaluated independently by two pharmacist reviewers; each reviewer will independently assign a severity rating to each ADE and pADE.

Registry
clinicaltrials.gov
Start Date
October 2013
End Date
December 2014
Last Updated
3 years ago
Study Type
Observational
Sex
All

Investigators

Responsible Party
Principal Investigator
Principal Investigator

Stuart Beatty

Assistant Professor of Clinical Pharmacy

Ohio State University

Eligibility Criteria

Inclusion Criteria

  • Adult patients discharged from the hospital in the last 7 days and with more than two chronic conditions and significant obstacles to accessing care in an office setting are eligible for study participation

Exclusion Criteria

  • Adult patients able to access care in an office setting.
  • Adult patients discharged from the hospital greater than 7 days prior to the office visit.

Outcomes

Primary Outcomes

Hospital Readmission

Time Frame: 30 days

Secondary Outcomes

  • Emergency Department Visit(30 days)

Study Sites (1)

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